Device and method for real-time detection of aeropathogens

ABSTRACT

Disclosed herein are devices and methods for the real-time detection of aeropathogens. The device includes an aerosampler having an air inlet and at least one collector tube, a microfluidic system which includes a container, piping, a micro-pump for flowing a liquid, and a viral detection chamber. The viral detection chamber has an electrode which may be equipped with functionalized biosensors, a counter electrode, an electronic detection system connectable to the electrodes of the viral detection chamber, and an embedded electronic processing system for processing data from the electronic detection system.

FIELD OF THE INVENTION

The present invention relates to the detection of pathogens, including aeroviruses and aerobacteria, such as SIV (swine Influenza virus) and/or PRRSV (porcine respiratory and reproductive syndrome virus), and/or MH (Mycoplasma Hyopneumoniae) in any environments where swine herds might be exposed to, or other aeropathogens that affect human populations and/or various animal farm industries including poultry.

BACKGROUND

Simply defined, tiny droplets suspended in air and containing biological materials like viruses, bacteria, and fungi are called “bioaerosols”. For most animal species, the organ that is most sensitive to bioaerosol exposure is the respiratory tract system. Our respiratory system is efficient in removing aerosols, but if the particle size falls below a particular range or the particles highly concentrated, they can cause health effects. In fact, very small particles (≲5 μm) can reach the pulmonary alveolar and cause severe respiratory illnesses in humans and animals.

Furthermore, it has been recently demonstrated that transmission of SIV, PRRSV, and MH via bio-aerosol is more efficient than spread through contaminated environmental surfaces/fomites, and that transmission via aerosols now accounts for more than 53% of all infections. Given the right atmospheric conditions, aeropathogens such as the SIV, PRRSV, and MH bio-aerosols, have been shown to travel up to 9.2 km and 4.7 Km respectively, proving that long distance airborne transport of aeropathogens occurs.

Currently, all existing detection systems for aeropathogens require more than 16 hours for collecting and analyzing samples, and therefore are not suited for screening potential pathogen carriers. Furthermore, there is no commercially available instrument capable of measuring in real time the type and concentration of airborne viruses or airborne bacteria.

Objects

An object is to provide a device and a method for real-time detection of aeropathogens.

Real-time within the meaning of the present disclosure means that a detection result shall be available within half an hour, preferably within 15 minutes, most preferred within 5 minutes, from starting the detection procedure, namely the first air introduced into the aerosampler as explained below.

Another object is to provide a device and a method to identify specific aeropathogens.

Another object is to provide a device and a method to identify quantitatively the concentration of specific aeropathogens present in the air.

Still another object is to detect different aeropathogens simultaneously.

Still another object is to provide a device for detecting aeropathogens which device can be used multiple times by an automatic cleansing and refreshing system.

Still another object is to provide a device and method for detecting aeropathogens, which is easy to handle by medical laymen, such as farmers and custom executives.

SUMMARY

We disclose a device for real-time detection of aeropathogens comprising an aerosampler having an air inlet, a microfluidic system comprising at least one container, piping and at least one micro pump for flowing a liquid, at least one viral detection chamber, each of the at least one viral detection chambers having at least a working electrode apt to be equipped with functionalized biosensors and at least one counter electrode, at least one electronic detection system connectable to the electrodes of the at least one viral detection chamber, and an electronic processing system processing data receivable from the at least one electronic detection system.

In an embodiment, the aerosampler comprises an optional dust collector, a first aeropathogen collector tube, a second collector tube and an air pump conveying ambient air first through the dust collector, if any, then through the first and second collector tubes. The first collector tube is adapted to collect larger aerosol particles, preferably having a diameter from about 2 μm to about 10 μm, and the second collector tube is adapted to collect smaller aerosol particles, preferably having a diameter of up to 5 μm. The inlet to the collector tubes is eccentric to the tube axis and oblique versus the bottom of the tubes such that injected air moves centrifugally along the walls of the collector tubes and thereby throw entrained aerosol particles against the wall of the tubes. Such small particle collectors are known in the art as “reverse flow cyclones”, e.g. from U.S. Pat. Nos. 4,941,899 and 8,205,511. The dust collector preferably also works with centrifugal forces.

During collecting aerosol particles the walls of the collector tubes are preferably continuously wetted from the at least one liquid container. The wetting liquid (a suitable buffer liquid) collected in the collector tube is continuously or batchwise conveyed to the viral detection chamber.

The electrodes of the viral detection chamber are of noble metal such as Ag, Au, Pt, Ru or their alloys, preferably Au. The surface of the electrodes is preferably covered with a suitable binding agent for the aeropathogen to be detected, preferably with a self-assembled monolayer of aptamers specific to the aeropathogen to be detected.

The electrodes of the viral detection chamber are biased with a suitable voltage, preferably of between −300 mV and +50 mV and the response of the system in the range of 20 pA and 20 μA is measured by a lock-in phase amplification circuitry operating at low frequency, preferably below 400 Hz. Alternatively, ultra low noise DC current amplifiers can be used although more expensive than lock-in amplifiers operating in the same current range.

Preferably, several viral detection chambers are present in parallel, detecting either the same aeropathogen and averaging the result, or detecting different pathogens. Each viral detection chamber has an independent lock-in phase amplification circuitry. Preferably, the several lock-in phase amplification circuitries use one common oscillator. The measured data are stored and processed in a computer, e.g. compared with previously stored calibration data to identify presence and concentration of aeropathogens in the air introduced in the aerosampler.

Preferably, the device comprises a number of containers for storing and providing different liquids, such as the wetting liquid for the collector tubes, various cleaning liquids including deionized water, acids such as concentrated H₂SO₄, for cleaning the viral detection chamber, the pipes and the collector tubes, etc., and liquids for refreshing the electrode surfaces. The liquid from the containers may be conveyed by a common micropump and a common tube connected by a three-way valve to the tube connecting the collector tubes with the viral detection chamber, if the containers are provided with shut-valves, each.

Preferably the device comprises an additional container at the outlet side of the viral detection chamber, for collecting waste, namely used liquids. Waste liquids are conveyed to the waste container by an additional micropump.

Preferably, the pumps, valves, flow rates and the electronic detection systems are controlled by an embedded electronic system (electronic processing system), programmed to make the different elements act according to a preselected scheme.

The invention also comprises a method for real-time detection of aeropathogens by providing an aerosampler having an air inlet and comprising at least one collector tube, a microfluidic system comprising at least one container, piping and at least one pump for flowing a liquid, at least one viral detection chamber having at least two electrodes and being equipped with functionalized biosensors, at least one electronic detection system connectable to the electrodes of the at least one viral detection chamber, and an electronic processing system processing data receivable from the at least one electronic detection system, the method comprising moistening the walls of the at least one collector tube, introducing air into the aerosampler, collecting aeropathogens at the moist walls of the aerosampler, flowing moisture from the walls of the aerosampler to the viral detection chamber, detecting electric response between the electrodes of the viral detection chamber, and processing the electric response in the electronic processing system to identify the presence of aeropathogens in the air.

Aptamers

Aptamers are specific oligonucleotides composed of single stranded DNA (ssDNA) or RNA that bind to a wide range of targets specifically. Aptamers can be obtained using an in vitro selection procedure called Systematic Evolution of Ligands by EXponential enrichment (SELEX), that starts with the incubation of random oligonucleotide libraries with the desired target molecules, followed by the separation and amplification of bound oligonucleotides. By repeating this process, an enriched pool is obtained, which can be used as a starting library for the next round of selection to attain high specificity and affinity to the target molecules. In principle, aptamers can be selected for any given target, ranging from small molecules to large proteins and even cells. When aptamers bind small molecular targets, these get incorporated into the nucleic acid structure, buried within the binding pockets of aptamer structures. On the other hand, large molecules (e.g. proteins) are structurally more complicated, allowing aptamer interactions at various sites via hydrogen bonding, electrostatic interactions and shape complementarity. The production of aptamers is not costly, and they are very low in batch-to-batch variation compared to the antibodies produced in vivo. In addition, aptamers can be chemically synthesized, are thermally stable, and are suitable for long-term storage. With these advantages, aptamers with high specificity and affinity have been developed for a variety of targets, including proteins, small molecules, whole cells, and viruses. Aptamers are now been widely used in diverse fields, such as diagnostics, therapeutics, and biosensors. While aptasensors emerged only about 10 years ago, they have already found broad applications in both basic research and biomedical diagnostics.

Aptamer-based biosensors possess unprecedented advantages compared to biosensors using natural receptors such as antibodies and enzymes:

-   -   First, aptamers with high specificity and affinity can be         selected in vitro for any given target, ranging from small         molecules to large proteins and even cells, thus making it         possible to develop a wide range of aptamer based biosensors.     -   Second, aptamers, once selected, can be synthesized with high         reproducibility and purity from commercial sources. Also, in         contrast to protein-based antibodies or enzymes, DNA aptamers         are usually highly chemically stable.     -   Third, aptamers often undergo significant conformational changes         upon target binding. This offers great flexibility in design of         novel biosensors with high detection sensitivity and         selectivity.     -   Fourth, the small size of aptamers provides advantages over         antibodies: (i) a greater surface density of receptors and (ii)         multiple binding to target molecules for sandwich assays.

Aptamers can be attached to the solid support at either the 5′-end or the 3′ end. Particularly, gold is broadly used as the target. Direct attachment of aptamers to gold surfaces could be achieved by using a thiol-alkane linked to the aptamer sequence. The gold surface could also be functionalized and the type of chemistry selected is dependent on what type of terminal functional group is linked to the aptamer (i.e. amine, thiol or biotin termini).

Gold surfaces functionalized with self-assembled monolayers (SAMs) can address the nonspecific adsorption of aptamer to the surface. Avidin-biotin technology has also been exploited for aptamer immobilization. Strepavidin can be physically adsorbed or covalently immobilized onto the support and the method mainly requires incubation of the biotin-tethered aptamer with the modified substrate. Studies of the anti-thrombin aptamer revealed that this biocoating method gives best results regarding sensitivity compared to other immobilization strategies.

The invention preferably makes use of aptamers for binding the pathogens on the electrodes of the viral detection chamber.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an overall diagram of a preferred design of the device;

FIG. 2 shows a preferred design of the aerosampler;

FIGS. 3a and 3b show the preferred collector tubes in detail;

FIG. 4 shows the viral detection chamber;

FIG. 5 illustrates the construction of the viral detection chamber;

FIG. 6 shows the flow of the wetting fluid during continuous flow measurement;

FIG. 7 shows the cleaning procedure;

FIG. 8 shows schematically the binding mechanism of a virus to a gold electrode;

FIG. 9 shows a graph of a typical detection cycle as obtained by the present invention;

FIG. 10 shows examples of response of the system to different concentrations of a virus.

Equal numerals in different drawings designate the same functional elements.

DETAILED DESCRIPTION

With reference to FIG. 1, numeral 1 designates the aerosampler. A gas pump 13 sucks in air from the air inlet 11, preferably equipped with a dust collector 12. Within the aerosampler 1 small particle droplets entrained in the air are separated and collected as explained in in more detail with reference to FIGS. 2 and 3 below. Wetting liquid (buffer solution) is conveyed from container 2 by means of a micropump 21 into the aerosampler. The buffer solution with collected droplets is conveyed to the at least one viral detection chamber 4; shown are four viral detection chambers 4 in parallel, allowing for detecting four different aeropathogens simultaneously. To each of the viral detection chambers 4 is assigned an electronic detection system 5 with a common oscillator 6. The dashed lines represent electric connecting lines. Measured signals from the viral detection chamber 4 are electronically stored and processed in a computer 7. An assembly of liquid containers 3 containing liquids for cleaning, rinsing and refreshing may be included in the liquid circuit by three-way valve 31. These liquids may be conveyed by a micropump 91 (suction side of the pump) to the viral detection chamber 4 and after use to a waste container 9. Pump 91 also helps conveying the buffer solution from the aerosampler 1 to the viral detection chamber 4. Valve 92 is open when the detection scan is made with continuously flowing buffer solution through the viral detection chamber 4 and is closed when the detection scan is made batchwise, namely non-flowing buffer solution. All functions of the pumps, valves and electronic detection systems 5 are controlled via control lines 82 to controller (the embedded electronic system) 8 according to a preselected procedure. Preferably pump 92 provides a variable flow rate of from 15 nanoliters (nL) per minute to 15 μl per minute. Two pumps may be installed in parallel, one allowing high flow rates and the other low flow rates, which may be run alternatively.

With reference to FIG. 2, in a preferred embodiment air is conveyed by suction of pump 13 from air inlet 11 through micro-centrifuges 12, 15 and 16. Numeral 12 designates a durst filter. Preferably pump 13 is set at a flow rate of between 3.5 to 7.5 liters per minute (normal pressure). The dust outlet 17 may be equipped with a dust container 18 for collecting dust particles of diameter of above about 10 μm. The walls of the collector tubes 15 and 16 are wetted via line 22 from the wetting liquid container 2 (FIG. 1). Collector tube 15 preferably mainly collects particles with a diameter of from 2 μm to 10 μm, whereas collector tube 15 is adapted to collect particles mainly with diameter up to 5 μm. The wetting liquid having caught particles from the air collect on the bottom of the collector tubes 15 and 16 is conveyed via line 32 to the viral detection chamber 4. The collector tubes preferable have a total inner volume of between 1 ml and 2.5 ml.

FIG. 3a shows the airflow through the collector tubes 15 and 16. FIG. 3b shows collector tube 15 turned by 90° around its axis as compared to FIG. 3a . Air is injected in each case eccentrically and oblique to the bottom of the tube to create centrifugal force for separation of the particles entrained in the air.

FIG. 4 shows the viral detection chamber in detail. FIG. 4a ) shows a top view, FIG. 4b ) shows a side view and FIG. 4c ) shows a front view. The designation of top, side or front view is only for defining the relative position of FIGS. 4 a), 4 b) and 4 c. The viral detection chamber may be arranged in any position, e.g. the front view may be the upper wall. The viral detection chamber, generally designated with 4, comprises an inner cavity 41 within a housing 401, 402 with an inlet 42 and an outlet 43. The arrows indicate the flow direction of the fluid received from the aerosampler 1. Preferably, the cavity 41 has a volume of between 0.5 and 1.5 mm³. A volume of between 0.6 to 1 mm³ is particularly preferred. The cavity 41 has parallel upper and lower walls carrying a number of counter electrodes 44 and working electrodes 45 opposite to each other. Preferably counter electrodes 44 are larger than the working electrodes that are carrying the binding agent for the aeropathogens. The smaller electrodes are the working electrodes. The distance between the working electrodes and the opposite counter electrode preferably is between 30 μm and 50 μm. The diameter of the counter electrodes 44 is preferably between 50 μm and up to 100 μm. The diameter of the working electrodes is preferably between 0.4 to 0.7 times the diameter of the counter electrodes. Each pair of working electrode and the opposite counter electrode create an electric field which is perpendicular to the flow direction of liquid. The distance of neighbouring counter electrodes is 15 to 30 times larger than their diameter. The electrodes are connected to connector terminals 47 and 48 as will be explained with reference to FIG. 5. An additional electrode 46 with connector terminals 49 serves as reference electrode. There is no working electrode opposite to the reference electrode. During detection the working electrodes are at a variable biasing voltage of −370 and +50 mV against the counter electrodes.

The housing of the viral detection is composed of two plates of preferably borosilicate float glass 401 and 402. Two holes 42 and 43 are drilled through one of the plates 402. Then the cavity is prepared by a reactive ion-CF₄ plasma etch technique. It may be sufficient to provide a cavity in only one of the plates.

FIG. 5 a) and b) show the two plates 401 and 402 with their partial cavities on top. After providing the cavity 41, electrodes 44, 45 and 46, the connector terminals 47, 48 and 49 and the lines 441, 451 and 461 are applied to the plates by known photolithographic technique and deposition of noble metal vapour. The connecting lines 441, 451 and 461 are isolated by a suitable cover layer, e.g. of SiO₂. After removal of any organic material from the surface of the plates, the plates are aligned to each other as indicated by the dotted line 403 in FIG. 4c ). The exactly aligned plates 401 and 402 are then fused by heating to between about 500° C. and 650° C. under high pressure perpendicular to the fuse line 403.

FIG. 6 is a flow chart showing the flow of the wetting fluid from the moistening container to the waste container with flow rate controllers #1 and #2 cooperating with the controller 8.

FIG. 7 is a flow chart showing the cleaning/refreshing procedure. First (I) deionized water is conveyed through the device. Thereafter (II) cleaning liquid e.g. concentrated H₂SO₄ is flown through the viral detection chamber 4 from one of the containers 3, followed by rinsing with deionized water from another container 3. This may be repeated several times until constant current is measured from the electrodes of the viral detection chamber 4. Thereafter refreshing liquid is conveyed from another container 3. Refreshing liquid contains the functionalized aptamers (for a given aeropathogen) that will form the self-assembled monolayer on the working electrode.

FIG. 8 shows a typical binding mechanism for aeropathogens. First, the self-assembled monolayer on the working electrode is produced according known technique. In our initial experiments we used an amino- and thiol-modified aptamer having a methylene-blue reporter group in a 0.5 to about 1 μmolar aqueous buffer solution through the viral detection chamber. The formula of the self-assembled monolayer of aptamers was

5′-HS—(CH₂)₆-GCAGT APTAMER ACTGCT-(CH₂)₇—NH₂-MB-3′.

or

5′-MB-NH₂—(CH₂)₇-TCGTCA-APTAMER-TGACG-(CH₂)₆—HS-3′.

The left picture in FIG. 8 shows a single aptamer bound to a gold surface. The viral detection chamber is then rinsed with deionized water to remove the buffer solution.

Thereafter the liquid from the collector tubes is fed to the viral detection chamber. If aeropathogens are present in the liquid, what is indicated by the arrow and “virus” in the middle of FIG. 8, the aeropathogens binds to the aptamer by emitting an electron causing a response to the electronic detection system. After completion of the measurement, the viral detection chamber is rinsed with deionized water to remove all aeropathogens.

FIG. 9 shows a typical detection cycle, wherein the x-axis represents the bias-voltage and the y-axis represents the measured current. The upper solid curve obtained with no virus in the air is the calibration curve taken before each detection of ambient air. The lower dashed curve is obtained with viruses in the air. From the difference of areas below both curves, it is possible to estimate the concentration of virus in the air. Even if the aptamer is unspecific to the aeropathogen, information on the type of aeropathogen may be obtained from position of the maximum of the upper curve on the x-axis may. The upper dashed curve is obtained after removal of the aeropathogens of a previous detection for calibration for the next detection cycle.

FIG. 10 demonstrates preliminary experiments showing the electronic response of the system as a function of virus concentration. The detection chamber is first floated with a solution containing S1+H1N1-aptamers to cover the working electrodes with such aptamers. Then, deionized water is fed from one of the containers 3 to remove any buffer solution for 5 min (time 0-300 s of the diagram). Thereafter the biasing voltage is set to 235 mV for optimal binding and virus carrying air at a concentration of 200 nMol/l (represented as the concentration of Hemaggluttinin as measured by PCR=polymerase chain reaction)) is introduced into the aerosampler with continuous wetting the walls of the micro-centrifuges for another 5 min. The current drops to 7.5 nA, corresponding to a response of 1.8 nA. Then the supply of air is stopped, the biasing voltage is set to 100 mV and a BSL-solution (Phosphate Buffer Saline) with no viruses is injected from another container 3, whereby the viral particles are released from the sensors (“flush circle”) until the current returns to 9.3 nA. At the time of 900 s the BSL-solution is stopped and air with a virus concentration of 400 nMol/l is introduced into the aerosampler. The current now drops to 5.4 nA, corresponding to a response of 3.9 nA. Then this detection and flushing cycle is repeated. The last detection cycle is run with air containing 800 nMol/l viruses. The current drops to 0.8 nA, corresponding to a response of 8.5 nA. Accordingly, the response is nearly linear to the virus concentration in the air.

If after a number of detection/flushing cycles the current does not return to the original value (in the example 9.3 nA) the aptamers are removed from the detection chamber by flowing concentrated H₂SO₄ through the detection chamber with subsequent removing the acid with deionized water and renewing the aptamer coverage of the working electrodes.

In this preferred embodiment there are at least four containers 3 containing deionized water, BSL-solution, concentrated H₂SO₄ and a refreshing solution providing aptamers.

R&D resulting in this patent application has been funded in part by National Research Council of Canada (NRCC) and supported by NIOSH, Cincinnati, Ohio, USA, by providing the detailed drawings of the tandem reverse flow cyclones. 

I/We claim:
 1. A method for real-time detection of aeropathogens by providing an aerosampler having an air inlet and comprising at least one collector tube, a microfluidic system comprising at least one container, piping and at least one pump for flowing a liquid, at least one viral detection chamber, the at least one viral detection chamber having at least one working electrode being equipped with functionalized biosensors and at least one counter electrode, at least one electronic detection system connectable to the electrodes of the at least one viral detection chamber, and an electronic processing system processing data receivable from the at least one electronic detection system, the method comprising: moistening the walls of the at least one collector tube, introducing air into the aerosampler, collecting aeropathogens at the moist walls of the at least one collector tube, flowing moisture from the walls of the aerosampler to the viral detection chamber, detecting electric response between the electrodes of the viral detection chamber, and processing the electric response in the electronic processing system to identify the presence of aeropathogens in the air.
 2. The method according to claim 1, wherein two size distributions of aeropathogens particles and/or droplets are collected simultaneously with the aerosampler.
 3. The method according to claim 1, wherein the inner walls of the at least one collector tube is continuously wetted with an adequate biofluid for the targeted aeropathogens.
 4. The method according to claim 1, wherein the viral detection chamber can be repeatedly cleaned with pure H₂SO₄ acid without any damage or alteration after completion of the detection measurement.
 5. The method according to claim 1, provided with an electronic control system for controlling various cleaning procedures of the microfluidic system for the at least one viral detection chamber and rejuvenation procedures of the biosensors.
 6. The method according to claim 1, utilizing an electric field which is perpendicular to the flow of liquid through the at least one viral detection chamber.
 7. The method according to claim 1, wherein two to six viral detection chambers are operable in parallel to detect two to six aeropathogens simultaneously.
 8. The method according to claim 1, wherein all fluids used are collected in a waste container.
 9. The method according to claim 1, wherein the electronic processing system performs signal analysis and pattern recognition for the selected pathogens. 